Skip to Content
MilliporeSigma
All Photos(3)

Key Documents

View All Documentation

326712

Sigma-Aldrich

Ruthenium black

greener alternative

Synonym(s):

Ruthenium

Sign Into View Organizational & Contract Pricing

Select a Size

1 G
$143.45

$143.45

List Price$151.00Save 5%
Web-Only Promotion

Available to ship onApril 22, 2025Details

Request a Bulk Order
All Photos(3)

Select a Size

Change View
1 G
$143.45

About This Item

Empirical Formula (Hill Notation):
Ru
CAS Number:
7440-18-8
Molecular Weight:
101.07
EC Number:
231-127-1
MDL number:
MFCD00011207
UNSPSC Code:
12141739
PubChem Substance ID:
24859614
NACRES:
NA.23

$143.45

List Price$151.00Save 5%
Web-Only Promotion

Available to ship onApril 22, 2025Details

Request a Bulk Order

assay

≥98%

Quality Level

100

form

powder

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

resistivity

7.1 μΩ-cm, 0°C

surface area

17-26 m2/g

bp

3900 °C (lit.)

mp

2310 °C (lit.)

density

12.45 g/cm3 (lit.)

greener alternative category

, Enabling

SMILES string

[Ru]

InChI

1S/Ru

InChI key

KJTLSVCANCCWHF-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

Application

Ru based complexes may be used in the synthesis of anticancer drugs.[1] Ru complexes in conjunction with magnesium may be used in the atom transfer radical addition (ATRA) and cyclization (ATRC) reactions. [2]
Ru may be used as a catalyst in the following reactions;
  • oxidative coupling of indoles and pyrroles with several alkenes[3]
  • arylations reactions.[4]

Packaging

Packaged in glass bottles

Storage Class

4.1B - Flammable solid hazardous materials

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCX1622
MKCW0694
MKCW6420
MKCW4936
MKCV2501

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Lipeng Wu et al.
Journal of the American Chemical Society, 135(10), 3989-3996 (2013-02-20)
An efficient and regioselective ruthenium-catalyzed hydroaminomethlyation of olefins is reported. Key to success is the use of specific 2-phosphino-substituted imidazole ligands and triruthenium dodecacarbonyl as catalyst. Both industrially important aliphatic as well as various functionalized olefins react with primary and
M Beye et al.
Physical review letters, 110(18), 186101-186101 (2013-05-21)
We have studied the femtosecond dynamics following optical laser excitation of CO adsorbed on a Ru surface by monitoring changes in the occupied and unoccupied electronic structure using ultrafast soft x-ray absorption and emission. We recently reported [M. Dell'Angela et
Rafael E Rodríguez-Lugo et al.
Nature chemistry, 5(4), 342-347 (2013-03-21)
The development of an efficient catalytic process that mimics the enzymatic function of alcohol dehydrogenase is critical for using biomass alcohols for both the production of H2 as a chemical energy carrier and fine chemicals under waste-free conditions. Dehydrogenation of
Direct synthesis of pyrroles by dehydrogenative coupling of β-aminoalcohols with secondary alcohols catalyzed by ruthenium pincer complexes.
Dipankar Srimani et al.
Angewandte Chemie (International ed. in English), 52(14), 4012-4015 (2013-03-08)
Bin Li et al.
The Journal of organic chemistry, 78(18), 9345-9353 (2013-09-13)
An efficient ruthenium-catalyzed oxidative coupling of indoles and pyrroles with various alkenes at the C2-position assisted by employing the N,N-dimethylcarbamoyl moiety as a directing group is reported. The catalytic reaction proceeds in an excellent regio- and stereoselective manner.
View All Related Papers

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service